Canonical Allele Identifier: CA2335961506

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396177T= , CM000681.2:g.40396177T=	GRCh38
NC_000019.9:g.40902084T= , CM000681.1:g.40902084T=	GRCh37
NC_000019.8:g.45593924T=	NCBI36
NG_007979.1:g.22188A= , LRG_265:g.22188A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2175A= MANE Select	ENSP00000326018.6:p.Pro725=
ENST00000673881.1:c.1758A=	ENSP00000501070.1:p.Pro586=
ENST00000674005.2:c.2460A=	ENSP00000501261.1:p.Pro820=
ENST00000674773.1:c.1758A=	ENSP00000502579.1:p.Pro586=
ENST00000675517.1:c.2050A=
ENST00000676076.1:c.2036A=
ENST00000676260.1:c.2137A=
ENST00000676316.1:c.2062A=
ENST00000291825.11:c.*2380A=	ENSP00000291825.6:n.*2380A=
ENST00000324001.7:c.2175A=	ENSP00000326018.6:p.Pro725=
NM_020956.2:c.*2380A= , LRG_265t1:c.*2380A=	NP_066007.1:n.*2380A=
NM_181882.2:c.2175A= , LRG_265t2:c.2175A=	NP_870998.2:p.Pro725=
XM_011527171.1:c.2175A=	XP_011525473.1:p.Pro725=
XM_011527171.2:c.2175A=	XP_011525473.1:p.Pro725=
XM_017027046.1:c.2073A=	XP_016882535.1:p.Pro691=
XM_017027047.1:c.2073A=	XP_016882536.1:p.Pro691=
NM_181882.3:c.2175A= MANE Select	NP_870998.2:p.Pro725=